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Showing results (131-140 of 143) with videos related to

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Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
Neuromuscular Disorders : NMD|October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The NetherlandsF Muntoni, E Bertini, C Bönnemann, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 8, 2013
Diagnostic measures for sarcopenia and bone mineral densityA Y Bijlsma, M C G Meskers, M Molendijk, et al.
Age (Dordrecht, Netherlands)|July 3, 2013
Diagnostic criteria for sarcopenia and physical performanceA Y Bijlsma, C G M Meskers, N van den Eshof, et al.
Neuromuscular Disorders : NMD|March 11, 2019
Respiratory and upper limb function as outcome measures in ambulant and non-ambulant subjects with Duchenne muscular dystrophy: A prospective multicentre studyV Ricotti, V Selby, D Ridout, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Orphanet Journal of Rare Diseases|May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patientsC I van Capelle, J C van der Meijden, J M P van den Hout, et al.
Neuromuscular Disorders : NMD|August 19, 2003
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)F Muntoni, B Valero de Bernabe, R Bittner, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, et al.
Pageof 15

Showing results (131-140 of 143) with videos related to

Sort By:
Pageof 15
Neuromuscular Disorders : NMD|October 6, 2005
134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The NetherlandsE Bertini, A Burghes, K Bushby, et al.
Neuromuscular Disorders : NMD|October 26, 2002
98th ENMC International Workshop on Congenital Muscular Dystrophy (CMD), 7th Workshop of the International Consortium on CMD, 2nd Workshop of the MYO CLUSTER project GENRE. 26-28th October, 2001, Naarden, The NetherlandsF Muntoni, E Bertini, C Bönnemann, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 8, 2013
Diagnostic measures for sarcopenia and bone mineral densityA Y Bijlsma, M C G Meskers, M Molendijk, et al.
Age (Dordrecht, Netherlands)|July 3, 2013
Diagnostic criteria for sarcopenia and physical performanceA Y Bijlsma, C G M Meskers, N van den Eshof, et al.
Neuromuscular Disorders : NMD|March 11, 2019
Respiratory and upper limb function as outcome measures in ambulant and non-ambulant subjects with Duchenne muscular dystrophy: A prospective multicentre studyV Ricotti, V Selby, D Ridout, et al.
Human Molecular Genetics|December 14, 2001
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1CM Brockington, Y Yuva, P Prandini, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Orphanet Journal of Rare Diseases|May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patientsC I van Capelle, J C van der Meijden, J M P van den Hout, et al.
Neuromuscular Disorders : NMD|August 19, 2003
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)F Muntoni, B Valero de Bernabe, R Bittner, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, et al.
Pageof 15